A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14800697



Internal ID3926658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75900866..75977307hg38UCSC Ensembl
chr13:76475002..76551443hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3876442
hg1976442
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3632756
Supporting Variants
SamplesHG03578
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14800697
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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